PD 166326 Struktur

PD 166326

Bezeichnung:PD 166326

CAS-Nr185039-91-2

Englisch Name:PD 166326

CBNumberCB22591977

SummenformelC21H16Cl2N4O2

Molgewicht427.28

MOL-Datei185039-91-2.mol

PD 166326 physikalisch-chemischer Eigenschaften

Siedepunkt	646.3±65.0 °C(Predicted)
Dichte	1.475±0.06 g/cm3(Predicted)
storage temp.	Store at -20°C
Löslichkeit	≤25mg/ml in DMSO;25mg/ml in dimethyl formamide
Aggregatzustand	crystalline solid
pka	14.29±0.10(Predicted)
Farbe	White to off-white

PD 166326 Chemische Eigenschaften,Einsatz,Produktion Methoden

Biologische Aktivität
pd 166326 is a receptor tyrosine kinase inhibitor.receptor tyrosine kinases are the high-affinity cell surface receptors for many growth factors, cytokines, as well as hormones. they have been shown not only to be critical regulators of normal cellular processes but also to have a key role in the development of many types of cancer.
in vitro
pd 166326 was identified as a pyridopyrimidine-type inhibitor of receptor tyrosine kinases inhibiting c-abl and bcr/abl-dependent cell growth. in addition, pd 166326 could also potently inhibit c-src. moreover, pd166326 was found to be superior to imatinib mesylate in inhibiting the constitutive tyrosine phosphorylation of numerous leukemia-cell proteins, such as the src family member lyn [1, 2].
in vivo
in mice with the cml-like disease, pd166326 could rapidly inhibit bcr/abl kinase activity after a single po dose and showed great antileukemic activity. it was found that 70% of pd166326-treated mice achieved a white blood cell count less than 20.0 × 109/l at necropsy, compared with 8% of imatinib mesylate–treated animals. furthermore, 2/3 of pd166326-treated mice had complete resolution of splenomegaly, compared with none of the imatinib mesylate–treated animals. in addition, pd166326 could also prolong the survival of mice with imatinib mesylate–resistant cml induced by the bcr/abl mutants of p210/h396p and p210/m351t [2].
IC 50
8 nm for c-abl
Einzelnachweise
[1] wisniewski, d. ,lambek, c.l.,liu, c., et al. characterization of potent inhibitors of the bcr-abl and the c-kit receptor tyrosine kinases. cancer research 62(15), 4244-4255 (2002).
[2] wolff, n. c.,veach, d.r.,tong, w.p., et al. pd166326, a novel tyrosine kinase inhibitor, has greater antileukemic activity than imatinib mesylate in a murine model of chronic myeloid leukemia. blood 105(10), 3995-4003 (2005).

PD 166326 Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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